Canonical Allele Identifier: CA1920112744
Gene: ADK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.74589296T= , CM000672.2:g.74589296T= GRCh38
NC_000010.10:g.76349054T= , CM000672.1:g.76349054T= GRCh37
NC_000010.9:g.76019060T= NCBI36
NG_030484.1:g.443112T=
NG_030484.2:g.443112T=

Transcript Alleles

HGVS Amino-acid Change
NM_006721.4:c.741T= MANE Select NP_006712.2:p.Phe247=
ENST00000539909.6:c.741T= MANE Select ENSP00000443965.2:p.Phe247=
NM_001123.3:c.690T= NP_001114.2:p.Phe230=
NM_001123.4:c.690T= NP_001114.2:p.Phe230=
NM_001202449.1:c.636T= NP_001189378.1:p.Phe212=
NM_001202449.2:c.636T= NP_001189378.1:p.Phe212=
NM_001202450.1:c.570T= NP_001189379.1:p.Phe190=
NM_001202450.2:c.570T= NP_001189379.1:p.Phe190=
NM_001369123.1:c.741T= NP_001356052.1:p.Phe247=
NM_001369124.1:c.519T= NP_001356053.1:p.Phe173=
NM_006721.3:c.741T= NP_006712.2:p.Phe247=
ENST00000286621.6:c.741T= ENSP00000286621.2:p.Phe247=
ENST00000286621.7:c.741T= ENSP00000286621.3:p.Phe247=
ENST00000372734.3:c.690T= ENSP00000361819.3:p.Phe230=
ENST00000372734.5:c.690T= ENSP00000361819.3:p.Phe230=
ENST00000539909.5:c.570T= ENSP00000443965.1:p.Phe190=
ENST00000541550.5:c.636T= ENSP00000438321.1:p.Phe212=
ENST00000541550.6:c.690T= ENSP00000438321.2:p.Phe230=
ENST00000672394.1:c.465T= ENSP00000500390.1:p.Phe155=
ENST00000672429.1:c.570T= ENSP00000500292.1:p.Phe190=
ENST00000672604.1:c.481T=
ENST00000672920.1:c.*486T= ENSP00000500141.1:n.*486T=
ENST00000673027.1:c.636T= ENSP00000500201.1:p.Phe212=
ENST00000673310.1:c.*334T= ENSP00000500097.1:n.*334T=
ENST00000673352.1:c.741T= ENSP00000500056.1:p.Phe247=
XM_011539297.1:c.657T= XP_011537599.1:p.Phe219=
XM_017015698.1:c.741T= XP_016871187.1:p.Phe247=
XM_017015699.1:c.546T= XP_016871188.1:p.Phe182=
XM_017015700.1:c.741T= XP_016871189.1:p.Phe247=
XM_017015701.1:c.519T= XP_016871190.1:p.Phe173=
XM_017015702.1:c.690T= XP_016871191.1:p.Phe230=
XM_017015703.2:c.465T= XP_016871192.1:p.Phe155=
XM_017015705.1:c.570T= XP_016871194.1:p.Phe190=